Loading…

mTOR complexes differentially orchestrates eosinophil development in allergy

Eosinophil infiltration is considered a hallmark in allergic airway inflammation, and the blockade of eosinophil differentiation may be an effective approach for treating eosinophil-related disorders. Mammalian target of rapamycin (mTOR) is a vital modulator in cell growth control and related diseas...

Full description

Saved in:
Bibliographic Details
Published in:Scientific reports 2018-05, Vol.8 (1), p.6883-14, Article 6883
Main Authors: Zhu, Chen, Xia, Lixia, Li, Fei, Zhou, Lingren, Weng, Qingyu, Li, Zhouyang, Wu, Yinfang, Mao, Yuanyuan, Zhang, Chao, Wu, Yanping, Li, Miao, Ying, Songmin, Chen, Zhihua, Shen, Huahao, Li, Wen
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c540t-d1cbb7fa2b86954a24ecdabfb6d2c6a80083f695e1c76fcc054b5ff90886bbe63
cites cdi_FETCH-LOGICAL-c540t-d1cbb7fa2b86954a24ecdabfb6d2c6a80083f695e1c76fcc054b5ff90886bbe63
container_end_page 14
container_issue 1
container_start_page 6883
container_title Scientific reports
container_volume 8
creator Zhu, Chen
Xia, Lixia
Li, Fei
Zhou, Lingren
Weng, Qingyu
Li, Zhouyang
Wu, Yinfang
Mao, Yuanyuan
Zhang, Chao
Wu, Yanping
Li, Miao
Ying, Songmin
Chen, Zhihua
Shen, Huahao
Li, Wen
description Eosinophil infiltration is considered a hallmark in allergic airway inflammation, and the blockade of eosinophil differentiation may be an effective approach for treating eosinophil-related disorders. Mammalian target of rapamycin (mTOR) is a vital modulator in cell growth control and related diseases, and we have recently demonstrated that rapamycin can suppress eosinophil differentiation in allergic airway inflammation. Considering its critical role in haematopoiesis, we further investigated the role of mTOR in eosinophil differentiation in the context of asthmatic pathogenesis. Intriguingly, the inhibition of mTOR, either by genetic deletion or by another pharmacological inhibitor torin-1, accelerated the eosinophil development in the presence of IL-5. However, this was not observed to have any considerable effect on eosinophil apoptosis. The effect of mTOR in eosinophil differentiation was mediated by Erk signalling. Moreover, myeloid specific knockout of mTOR or Rheb further augmented allergic airway inflammation in mice after allergen exposure. Ablation of mTOR in myeloid cells also resulted in an increased number of eosinophil lineage-committed progenitors (Eops) in allergic mice. Collectively, our data uncovered the differential effects of mTOR in the regulation of eosinophil development, likely due to the distinct functions of mTOR complex 1 or 2, which thus exerts a pivotal implication in eosinophil-associated diseases.
doi_str_mv 10.1038/s41598-018-25358-z
format article
fullrecord <record><control><sourceid>proquest_doaj_</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_8bde9769a15a4d41966a45c2a91f6541</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><doaj_id>oai_doaj_org_article_8bde9769a15a4d41966a45c2a91f6541</doaj_id><sourcerecordid>2033742998</sourcerecordid><originalsourceid>FETCH-LOGICAL-c540t-d1cbb7fa2b86954a24ecdabfb6d2c6a80083f695e1c76fcc054b5ff90886bbe63</originalsourceid><addsrcrecordid>eNp9kV1rFDEUhgdRbKn9A17IgDfejOZ7khtBih-FhYLU65BkTnazZCZjMlvc_nqz3VpbL8xNQt4n78k5b9O8xug9RlR-KAxzJTuEZUc45bK7fdacEsR4Ryghzx-dT5rzUraoLk4Uw-plc0JUT5Ag-LRZjddX31uXxjnCLyjtELyHDNMSTIz7NmW3gbJks1QNUglTmjchtgPcQEzzWME2TG1lIa_3r5oX3sQC5_f7WfPjy-fri2_d6urr5cWnVec4Q0s3YGdt7w2xUijODGHgBmO9FQNxwkiEJPVVAex64Z1DnFnuvUJSCmtB0LPm8ug7JLPVcw6jyXudTNB3FymvtclLcBG0tAOoXiiDuWFD7V4Iw7gjRmEvOMPV6-PRa97ZEQZXO8omPjF9qkxho9fpRnNFCeK8Gry7N8jp564OS4-hOIjRTJB2RRNEGVEU8UOtt_-g27TLUx3VgaJ95ZSsFDlSLqdSMviHz2CkD9nrY_a6Zq_vste39dGbx208PPmTdAXoEShVmtaQ_9b-j-1vdhK8LQ</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2033742998</pqid></control><display><type>article</type><title>mTOR complexes differentially orchestrates eosinophil development in allergy</title><source>PubMed Central (Open Access)</source><source>Publicly Available Content Database</source><source>Free Full-Text Journals in Chemistry</source><source>Springer Nature - nature.com Journals - Fully Open Access</source><creator>Zhu, Chen ; Xia, Lixia ; Li, Fei ; Zhou, Lingren ; Weng, Qingyu ; Li, Zhouyang ; Wu, Yinfang ; Mao, Yuanyuan ; Zhang, Chao ; Wu, Yanping ; Li, Miao ; Ying, Songmin ; Chen, Zhihua ; Shen, Huahao ; Li, Wen</creator><creatorcontrib>Zhu, Chen ; Xia, Lixia ; Li, Fei ; Zhou, Lingren ; Weng, Qingyu ; Li, Zhouyang ; Wu, Yinfang ; Mao, Yuanyuan ; Zhang, Chao ; Wu, Yanping ; Li, Miao ; Ying, Songmin ; Chen, Zhihua ; Shen, Huahao ; Li, Wen</creatorcontrib><description>Eosinophil infiltration is considered a hallmark in allergic airway inflammation, and the blockade of eosinophil differentiation may be an effective approach for treating eosinophil-related disorders. Mammalian target of rapamycin (mTOR) is a vital modulator in cell growth control and related diseases, and we have recently demonstrated that rapamycin can suppress eosinophil differentiation in allergic airway inflammation. Considering its critical role in haematopoiesis, we further investigated the role of mTOR in eosinophil differentiation in the context of asthmatic pathogenesis. Intriguingly, the inhibition of mTOR, either by genetic deletion or by another pharmacological inhibitor torin-1, accelerated the eosinophil development in the presence of IL-5. However, this was not observed to have any considerable effect on eosinophil apoptosis. The effect of mTOR in eosinophil differentiation was mediated by Erk signalling. Moreover, myeloid specific knockout of mTOR or Rheb further augmented allergic airway inflammation in mice after allergen exposure. Ablation of mTOR in myeloid cells also resulted in an increased number of eosinophil lineage-committed progenitors (Eops) in allergic mice. Collectively, our data uncovered the differential effects of mTOR in the regulation of eosinophil development, likely due to the distinct functions of mTOR complex 1 or 2, which thus exerts a pivotal implication in eosinophil-associated diseases.</description><identifier>ISSN: 2045-2322</identifier><identifier>EISSN: 2045-2322</identifier><identifier>DOI: 10.1038/s41598-018-25358-z</identifier><identifier>PMID: 29720621</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>13/1 ; 13/100 ; 13/106 ; 13/31 ; 38/77 ; 64/60 ; 692/4017 ; 692/699/1785/31 ; 82/80 ; 96/21 ; Allergens ; Allergies ; Apoptosis ; Asthma ; Clonal deletion ; Humanities and Social Sciences ; Inflammation ; Interleukin 5 ; Leukocytes (eosinophilic) ; multidisciplinary ; Myeloid cells ; Rapamycin ; Respiratory tract ; Respiratory tract diseases ; Science ; Science (multidisciplinary) ; TOR protein</subject><ispartof>Scientific reports, 2018-05, Vol.8 (1), p.6883-14, Article 6883</ispartof><rights>The Author(s) 2018</rights><rights>2018. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c540t-d1cbb7fa2b86954a24ecdabfb6d2c6a80083f695e1c76fcc054b5ff90886bbe63</citedby><cites>FETCH-LOGICAL-c540t-d1cbb7fa2b86954a24ecdabfb6d2c6a80083f695e1c76fcc054b5ff90886bbe63</cites><orcidid>0000-0003-1770-8956 ; 0000-0002-7721-0175</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2033742998/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2033742998?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29720621$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhu, Chen</creatorcontrib><creatorcontrib>Xia, Lixia</creatorcontrib><creatorcontrib>Li, Fei</creatorcontrib><creatorcontrib>Zhou, Lingren</creatorcontrib><creatorcontrib>Weng, Qingyu</creatorcontrib><creatorcontrib>Li, Zhouyang</creatorcontrib><creatorcontrib>Wu, Yinfang</creatorcontrib><creatorcontrib>Mao, Yuanyuan</creatorcontrib><creatorcontrib>Zhang, Chao</creatorcontrib><creatorcontrib>Wu, Yanping</creatorcontrib><creatorcontrib>Li, Miao</creatorcontrib><creatorcontrib>Ying, Songmin</creatorcontrib><creatorcontrib>Chen, Zhihua</creatorcontrib><creatorcontrib>Shen, Huahao</creatorcontrib><creatorcontrib>Li, Wen</creatorcontrib><title>mTOR complexes differentially orchestrates eosinophil development in allergy</title><title>Scientific reports</title><addtitle>Sci Rep</addtitle><addtitle>Sci Rep</addtitle><description>Eosinophil infiltration is considered a hallmark in allergic airway inflammation, and the blockade of eosinophil differentiation may be an effective approach for treating eosinophil-related disorders. Mammalian target of rapamycin (mTOR) is a vital modulator in cell growth control and related diseases, and we have recently demonstrated that rapamycin can suppress eosinophil differentiation in allergic airway inflammation. Considering its critical role in haematopoiesis, we further investigated the role of mTOR in eosinophil differentiation in the context of asthmatic pathogenesis. Intriguingly, the inhibition of mTOR, either by genetic deletion or by another pharmacological inhibitor torin-1, accelerated the eosinophil development in the presence of IL-5. However, this was not observed to have any considerable effect on eosinophil apoptosis. The effect of mTOR in eosinophil differentiation was mediated by Erk signalling. Moreover, myeloid specific knockout of mTOR or Rheb further augmented allergic airway inflammation in mice after allergen exposure. Ablation of mTOR in myeloid cells also resulted in an increased number of eosinophil lineage-committed progenitors (Eops) in allergic mice. Collectively, our data uncovered the differential effects of mTOR in the regulation of eosinophil development, likely due to the distinct functions of mTOR complex 1 or 2, which thus exerts a pivotal implication in eosinophil-associated diseases.</description><subject>13/1</subject><subject>13/100</subject><subject>13/106</subject><subject>13/31</subject><subject>38/77</subject><subject>64/60</subject><subject>692/4017</subject><subject>692/699/1785/31</subject><subject>82/80</subject><subject>96/21</subject><subject>Allergens</subject><subject>Allergies</subject><subject>Apoptosis</subject><subject>Asthma</subject><subject>Clonal deletion</subject><subject>Humanities and Social Sciences</subject><subject>Inflammation</subject><subject>Interleukin 5</subject><subject>Leukocytes (eosinophilic)</subject><subject>multidisciplinary</subject><subject>Myeloid cells</subject><subject>Rapamycin</subject><subject>Respiratory tract</subject><subject>Respiratory tract diseases</subject><subject>Science</subject><subject>Science (multidisciplinary)</subject><subject>TOR protein</subject><issn>2045-2322</issn><issn>2045-2322</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNp9kV1rFDEUhgdRbKn9A17IgDfejOZ7khtBih-FhYLU65BkTnazZCZjMlvc_nqz3VpbL8xNQt4n78k5b9O8xug9RlR-KAxzJTuEZUc45bK7fdacEsR4Ryghzx-dT5rzUraoLk4Uw-plc0JUT5Ag-LRZjddX31uXxjnCLyjtELyHDNMSTIz7NmW3gbJks1QNUglTmjchtgPcQEzzWME2TG1lIa_3r5oX3sQC5_f7WfPjy-fri2_d6urr5cWnVec4Q0s3YGdt7w2xUijODGHgBmO9FQNxwkiEJPVVAex64Z1DnFnuvUJSCmtB0LPm8ug7JLPVcw6jyXudTNB3FymvtclLcBG0tAOoXiiDuWFD7V4Iw7gjRmEvOMPV6-PRa97ZEQZXO8omPjF9qkxho9fpRnNFCeK8Gry7N8jp564OS4-hOIjRTJB2RRNEGVEU8UOtt_-g27TLUx3VgaJ95ZSsFDlSLqdSMviHz2CkD9nrY_a6Zq_vste39dGbx208PPmTdAXoEShVmtaQ_9b-j-1vdhK8LQ</recordid><startdate>20180502</startdate><enddate>20180502</enddate><creator>Zhu, Chen</creator><creator>Xia, Lixia</creator><creator>Li, Fei</creator><creator>Zhou, Lingren</creator><creator>Weng, Qingyu</creator><creator>Li, Zhouyang</creator><creator>Wu, Yinfang</creator><creator>Mao, Yuanyuan</creator><creator>Zhang, Chao</creator><creator>Wu, Yanping</creator><creator>Li, Miao</creator><creator>Ying, Songmin</creator><creator>Chen, Zhihua</creator><creator>Shen, Huahao</creator><creator>Li, Wen</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><general>Nature Portfolio</general><scope>C6C</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0003-1770-8956</orcidid><orcidid>https://orcid.org/0000-0002-7721-0175</orcidid></search><sort><creationdate>20180502</creationdate><title>mTOR complexes differentially orchestrates eosinophil development in allergy</title><author>Zhu, Chen ; Xia, Lixia ; Li, Fei ; Zhou, Lingren ; Weng, Qingyu ; Li, Zhouyang ; Wu, Yinfang ; Mao, Yuanyuan ; Zhang, Chao ; Wu, Yanping ; Li, Miao ; Ying, Songmin ; Chen, Zhihua ; Shen, Huahao ; Li, Wen</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c540t-d1cbb7fa2b86954a24ecdabfb6d2c6a80083f695e1c76fcc054b5ff90886bbe63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>13/1</topic><topic>13/100</topic><topic>13/106</topic><topic>13/31</topic><topic>38/77</topic><topic>64/60</topic><topic>692/4017</topic><topic>692/699/1785/31</topic><topic>82/80</topic><topic>96/21</topic><topic>Allergens</topic><topic>Allergies</topic><topic>Apoptosis</topic><topic>Asthma</topic><topic>Clonal deletion</topic><topic>Humanities and Social Sciences</topic><topic>Inflammation</topic><topic>Interleukin 5</topic><topic>Leukocytes (eosinophilic)</topic><topic>multidisciplinary</topic><topic>Myeloid cells</topic><topic>Rapamycin</topic><topic>Respiratory tract</topic><topic>Respiratory tract diseases</topic><topic>Science</topic><topic>Science (multidisciplinary)</topic><topic>TOR protein</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhu, Chen</creatorcontrib><creatorcontrib>Xia, Lixia</creatorcontrib><creatorcontrib>Li, Fei</creatorcontrib><creatorcontrib>Zhou, Lingren</creatorcontrib><creatorcontrib>Weng, Qingyu</creatorcontrib><creatorcontrib>Li, Zhouyang</creatorcontrib><creatorcontrib>Wu, Yinfang</creatorcontrib><creatorcontrib>Mao, Yuanyuan</creatorcontrib><creatorcontrib>Zhang, Chao</creatorcontrib><creatorcontrib>Wu, Yanping</creatorcontrib><creatorcontrib>Li, Miao</creatorcontrib><creatorcontrib>Ying, Songmin</creatorcontrib><creatorcontrib>Chen, Zhihua</creatorcontrib><creatorcontrib>Shen, Huahao</creatorcontrib><creatorcontrib>Li, Wen</creatorcontrib><collection>Springer Nature OA Free Journals</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest Health and Medical</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>ProQuest Science Journals</collection><collection>ProQuest Biological Science Journals</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Directory of Open Access Journals</collection><jtitle>Scientific reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhu, Chen</au><au>Xia, Lixia</au><au>Li, Fei</au><au>Zhou, Lingren</au><au>Weng, Qingyu</au><au>Li, Zhouyang</au><au>Wu, Yinfang</au><au>Mao, Yuanyuan</au><au>Zhang, Chao</au><au>Wu, Yanping</au><au>Li, Miao</au><au>Ying, Songmin</au><au>Chen, Zhihua</au><au>Shen, Huahao</au><au>Li, Wen</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>mTOR complexes differentially orchestrates eosinophil development in allergy</atitle><jtitle>Scientific reports</jtitle><stitle>Sci Rep</stitle><addtitle>Sci Rep</addtitle><date>2018-05-02</date><risdate>2018</risdate><volume>8</volume><issue>1</issue><spage>6883</spage><epage>14</epage><pages>6883-14</pages><artnum>6883</artnum><issn>2045-2322</issn><eissn>2045-2322</eissn><abstract>Eosinophil infiltration is considered a hallmark in allergic airway inflammation, and the blockade of eosinophil differentiation may be an effective approach for treating eosinophil-related disorders. Mammalian target of rapamycin (mTOR) is a vital modulator in cell growth control and related diseases, and we have recently demonstrated that rapamycin can suppress eosinophil differentiation in allergic airway inflammation. Considering its critical role in haematopoiesis, we further investigated the role of mTOR in eosinophil differentiation in the context of asthmatic pathogenesis. Intriguingly, the inhibition of mTOR, either by genetic deletion or by another pharmacological inhibitor torin-1, accelerated the eosinophil development in the presence of IL-5. However, this was not observed to have any considerable effect on eosinophil apoptosis. The effect of mTOR in eosinophil differentiation was mediated by Erk signalling. Moreover, myeloid specific knockout of mTOR or Rheb further augmented allergic airway inflammation in mice after allergen exposure. Ablation of mTOR in myeloid cells also resulted in an increased number of eosinophil lineage-committed progenitors (Eops) in allergic mice. Collectively, our data uncovered the differential effects of mTOR in the regulation of eosinophil development, likely due to the distinct functions of mTOR complex 1 or 2, which thus exerts a pivotal implication in eosinophil-associated diseases.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>29720621</pmid><doi>10.1038/s41598-018-25358-z</doi><tpages>14</tpages><orcidid>https://orcid.org/0000-0003-1770-8956</orcidid><orcidid>https://orcid.org/0000-0002-7721-0175</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 2045-2322
ispartof Scientific reports, 2018-05, Vol.8 (1), p.6883-14, Article 6883
issn 2045-2322
2045-2322
language eng
recordid cdi_doaj_primary_oai_doaj_org_article_8bde9769a15a4d41966a45c2a91f6541
source PubMed Central (Open Access); Publicly Available Content Database; Free Full-Text Journals in Chemistry; Springer Nature - nature.com Journals - Fully Open Access
subjects 13/1
13/100
13/106
13/31
38/77
64/60
692/4017
692/699/1785/31
82/80
96/21
Allergens
Allergies
Apoptosis
Asthma
Clonal deletion
Humanities and Social Sciences
Inflammation
Interleukin 5
Leukocytes (eosinophilic)
multidisciplinary
Myeloid cells
Rapamycin
Respiratory tract
Respiratory tract diseases
Science
Science (multidisciplinary)
TOR protein
title mTOR complexes differentially orchestrates eosinophil development in allergy
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-27T18%3A03%3A41IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_doaj_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=mTOR%20complexes%20differentially%20orchestrates%20eosinophil%20development%20in%20allergy&rft.jtitle=Scientific%20reports&rft.au=Zhu,%20Chen&rft.date=2018-05-02&rft.volume=8&rft.issue=1&rft.spage=6883&rft.epage=14&rft.pages=6883-14&rft.artnum=6883&rft.issn=2045-2322&rft.eissn=2045-2322&rft_id=info:doi/10.1038/s41598-018-25358-z&rft_dat=%3Cproquest_doaj_%3E2033742998%3C/proquest_doaj_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c540t-d1cbb7fa2b86954a24ecdabfb6d2c6a80083f695e1c76fcc054b5ff90886bbe63%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2033742998&rft_id=info:pmid/29720621&rfr_iscdi=true